Macrophage-independent fungicidal action of the pulmonary collectins

J Biol Chem. 2003 Sep 19;278(38):36250-6. doi: 10.1074/jbc.M303086200. Epub 2003 Jul 11.

Abstract

Histoplasma capsulatum (Hc) is a facultative intracellular fungal pathogen that causes acute and chronic pneumonia. In this study, we investigated the role of the pulmonary collectins, surfactant proteins (SP) A and D, in the clearance of Hc yeast from the lung. Exposure of yeast to either collectin induced a dose-dependent decrease in [3H]leucine incorporation by several strains of Hc. This decrement was attributed to killing of the collectin-exposed yeast since it failed to grow on agar medium. Exposure to SP-A or -D resulted in increased yeast permeability based on a leak of protein from the organism and enhanced access of an impermeant substrate to intracellular alkaline phosphatase. Inbred and outbred SP-A null (-/-) mice were modestly more susceptible to pulmonary infection with Hc than strain and age-matched SP-A (+/+) control mice. The increase in susceptibility was associated with a decrement in the number of CD8+ cells in the lungs of SP-A-/- mice. Neither SP-A nor SP-D inhibited the growth of macrophage-internalized Hc. We conclude that the SP-A and SP-D are antimicrobial proteins that directly inhibit the growth of Hc by increasing permeability of the organism and that Hc gains asylum from collectin-mediated killing by rapid entry into pulmonary macrophages.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Agar / pharmacology
  • Alkaline Phosphatase / metabolism
  • Alleles
  • Animals
  • Cell Division
  • Collectins / pharmacology
  • Dose-Response Relationship, Drug
  • Flow Cytometry
  • Histoplasma / metabolism
  • Humans
  • Leukocytes / microbiology
  • Lung / cytology*
  • Lung / metabolism
  • Lung / microbiology*
  • Macrophages / metabolism*
  • Mice
  • Mice, Inbred C3H
  • Mice, Transgenic
  • Pulmonary Surfactant-Associated Protein A / physiology
  • Pulmonary Surfactant-Associated Protein D / physiology
  • Rats
  • Rats, Sprague-Dawley
  • Recombinant Proteins / chemistry
  • Spleen / metabolism
  • Stem Cells / metabolism
  • Time Factors

Substances

  • Collectins
  • Pulmonary Surfactant-Associated Protein A
  • Pulmonary Surfactant-Associated Protein D
  • Recombinant Proteins
  • Agar
  • Alkaline Phosphatase